Lv22
130 积分 2023-11-27 加入
HiFi long-read genomes for difficult-to-detect clinically relevant variants
1天前
已完结
Disease variant prediction with deep generative models of evolutionary data
5个月前
已完结
Epilepsy genetics: clinical impacts and biological insights
1年前
已完结
Mitochondrial DNA polymerase mutations: an ever expanding molecular and clinical spectrum
1年前
已完结
Understanding the genetics of human infertility
1年前
已完结
Gene and stem cell therapy for inherited cardiac arrhythmias
1年前
已完结
Sensitivity of mitochondrial DNA heteroplasmy detection using Next Generation Sequencing
1年前
已完结
Clinical characteristics and treatment of 50 cases of Blau syndrome in Japan confirmed by genetic analysis of the NOD2 mutation
1年前
已完结
Genetic and Clinical Features of Blau Syndrome among Chinese Patients with Uveitis
1年前
已完结
Molecular mechanisms of epistasis within and between genes
1年前
已完结
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